Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.
about
Paradigms of ribosome synthesis: Lessons learned from ribosomal proteinsRNA mimicry by the fap7 adenylate kinase in ribosome biogenesisMutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesThe evolutionarily conserved protein Las1 is required for pre-rRNA processing at both ends of ITS2Yeast polypeptide exit tunnel ribosomal proteins L17, L35 and L37 are necessary to recruit late-assembling factors required for 27SB pre-rRNA processing.Ribosomal proteins L7 and L8 function in concert with six A₃ assembly factors to propagate assembly of domains I and II of 25S rRNA in yeast 60S ribosomal subunitsRole of ribosomal protein mutations in tumor development (Review)Gradual processing of the ITS1 from the nucleolus to the cytoplasm during synthesis of the human 18S rRNANuclear LC3 Associates with Slowly Diffusing Complexes that Survey the NucleolusTwo orthogonal cleavages separate subunit RNAs in mouse ribosome biogenesisNotchless-dependent ribosome synthesis is required for the maintenance of adult hematopoietic stem cellsProteomic Analysis of Liver Proteins in a Rat Model of Chronic Restraint Stress-Induced DepressionA Ribosomopathy Reveals Decoding Defective Ribosomes Driving Human DysmorphismPrioritizing genes for X-linked diseases using population exome data.Poly(A)-specific ribonuclease is a nuclear ribosome biogenesis factor involved in human 18S rRNA maturation.Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families.The human nucleolar protein FTSJ3 associates with NIP7 and functions in pre-rRNA processingGermline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiencyInterrelationships between yeast ribosomal protein assembly events and transient ribosome biogenesis factors interactions in early pre-ribosomesRibosomal protein SA haploinsufficiency in humans with isolated congenital aspleniaThe emerging importance of ribosomal dysfunction in the pathogenesis of hematologic disorders.Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implicationsAnalysis of two human pre-ribosomal factors, bystin and hTsr1, highlights differences in evolution of ribosome biogenesis between yeast and mammals.Involvement of human ribosomal proteins in nucleolar structure and p53-dependent nucleolar stressElucidation of motifs in ribosomal protein S9 that mediate its nucleolar localization and binding to NPM1/nucleophosminLoss of nucleolar histone chaperone NPM1 triggers rearrangement of heterochromatin and synergizes with a deficiency in DNA methyltransferase DNMT3A to drive ribosomal DNA transcription.Identification and Expression Analysis of Ribosome Biogenesis Factor Co-orthologs in Solanum lycopersicum.An overview of pre-ribosomal RNA processing in eukaryotesRibosomal protein gene deletions in Diamond-Blackfan anemia.Reduced expression of the mouse ribosomal protein Rpl17 alters the diversity of mature ribosomes by enhancing production of shortened 5.8S rRNA.Determinants of mammalian nucleolar architecture.Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemiaMammalian HCA66 protein is required for both ribosome synthesis and centriole duplicationhUTP24 is essential for processing of the human rRNA precursor at site A1, but not at site A0Longevity GWAS Using the Drosophila Genetic Reference Panel.Ribosome biogenesis dysfunction leads to p53-mediated apoptosis and goblet cell differentiation of mouse intestinal stem/progenitor cellsComprehensive proteomic analysis of nonintegrin laminin receptor interacting proteinsFunctions of ribosomal proteins in assembly of eukaryotic ribosomes in vivo.Structure of a human pre-40S particle points to a role for RACK1 in the final steps of 18S rRNA processing.Human PDCD2L Is an Export Substrate of CRM1 That Associates with 40S Ribosomal Subunit Precursors.
P2860
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P2860
Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@ast
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@en
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@nl
type
label
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@ast
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@en
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@nl
prefLabel
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@ast
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@en
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@nl
P2093
P2860
P356
P1476
Functional dichotomy of riboso ...... malian 40S ribosomal subunits.
@en
P2093
Gwennaële Fichant
Marie-Françoise O'Donohue
Marlène Faubladier
Pierre-Emmanuel Gleizes
Valérie Choesmel
P2860
P304
P356
10.1083/JCB.201005117
P407
P577
2010-09-01T00:00:00Z